autosomal dominant distal hereditary motor neuronopathy 6 Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant distal hereditary motor neuronopathy 6 (DOID:0111210)
Alliance: disease page
Synonyms: distal hereditary motor neuronopathy type 2D; distal hereditary motor neuropathy type IID; distal spinal muscular atrophy with calf predominance; HMN2D; HMN IID
Alt IDs: OMIM:615575
Definition: A distal hereditary motor neuropathy that has_material_basis_in heterozygous mutation in the FBXO38 gene on 5q32.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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